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HRID 656883作成日:2026年10月26日

Toluene → 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-methoxyquinolin-2(1H)-one

https://huagongshe.com/reaction/656883

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物tert-butyl {1-[2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl]piperidin-4-yl}carbamateHCID 59371209—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物1-[2-(4-aminopiperidin-1-yl)ethyl]-7-methoxyquinolin-2(1H)-oneHCID 5939828954%

反応手順

1,1-Dimethylethyl (1-{2-[7-(methyloxy)-2-oxo-1(2H)-quinolinyl]ethyl}-4-piperidinyl)carbamate (2.25 g; 5.61 mmol) was dissolved in a mixture of chloroform (20 ml) and HCl (15 ml) and stirred at rt under argon for 1 hour. The salts were dissolved in MeOH and a small amount of toluene added, all the solvents were then removed. The residues were redissolved in MeOH and stirred with amberlyst ion exchange resin until a neutral pH was reached. The resin was filtered off and the solvent removed and the crude residues were purified by column chromatography on silica gel using a 0-20% 2M NH3:MeOH/DCM gradient, to give the desired product (900 mg; 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071592B2
出典データセットuspto-grants-2011_12
ORD IDord-38651200edb34560991f3e690c603ce7
出典メモuspto-grants-2011_12